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Issue 60, 2017
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A mechanistic study of ethanol transformation into ethene and acetaldehyde on an oxygenated Au-exchanged ZSM-5 zeolite

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Abstract

Ethanol transformation to ethene and acetaldehyde over low- and high-spin state oxygenated Au-exchanged ZSM-5 zeolite has been investigated using a well-validated density functional method, M06-L. The reaction initiates from the ethanol O–H bond dissociation leading to the formation the ethoxide–hydroxide intermediate with the activation energy of 9.5 kcal mol−1. This intermediate can be then decomposed to either ethene or acetaldehyde products. In the ethene production pathway, the decomposition of the ethoxide–hydroxide intermediate proceeds via the β-H–C scission with the activation energy of 40.5 kcal mol−1. For the acetaldehyde production pathway, the ethoxide–hydroxide intermediate transforms to acetaldehyde via α-H–C scission with the activation barrier of 10.6 kcal mol−1 which is significantly lower than the ethene pathway. The reaction rate for acetaldehyde formation is also found to be higher than the ethene one. The results suggest that the acetaldehyde product is thermodynamically and kinetically favored over ethene for the transformation of the ethanol on oxygenated Au-exchanged ZSM-5 zeolite.

Graphical abstract: A mechanistic study of ethanol transformation into ethene and acetaldehyde on an oxygenated Au-exchanged ZSM-5 zeolite

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Supplementary files

Article information


Submitted
06 Jun 2017
Accepted
27 Jul 2017
First published
02 Aug 2017

This article is Open Access

RSC Adv., 2017,7, 38052-38058
Article type
Paper

A mechanistic study of ethanol transformation into ethene and acetaldehyde on an oxygenated Au-exchanged ZSM-5 zeolite

Y. Injongkol, T. Maihom, S. Choomwattana, B. Boekfa and J. Limtrakul, RSC Adv., 2017, 7, 38052
DOI: 10.1039/C7RA06313J

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